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蜂毒素全氟碳纳米囊的制备及评价

Preparation and evaluation of melittin perfluorocarbon nanocapsules
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摘要 目的制备蜂毒素全氟碳纳米囊,考察其外观特征、粒径、Zeta电位、电镜形态、包封率及稳定性。方法以全氟碳为纳米核心,通过高压均质法制备蜂毒素纳米囊。采用透射电镜和激光粒度分析仪检测纳米颗粒形态、粒径及Zeta电位,双波长考马斯亮蓝法测定纳米颗粒载药包封率。将制备的蜂毒素全氟碳纳米囊乳液置于4℃下密封贮藏30 d,以纳米囊的粒径和包封率的变化作为指标,考察其稳定性。结果蜂毒素全氟碳纳米囊的平均粒径为84.41 nm,多分散系数为0.115,Zeta电位为-52.1 mV。采用双波长考马斯亮蓝法测定蜂毒素全氟碳纳米囊包封率,在吸收度及线性均良好的情况下,考马斯亮蓝法检测游离蜂毒素含量的检测范围为0.5~25 mg/L,该范围内线性良好,相关系数为0.9993,蜂毒素药物的包封率为(86.31±0.76)%(n=3),RSD<1%,稳定性良好。结论采用高压均质法制备蜂毒素全氟碳纳米囊的方法可行,经粒径、形态、包封率方面的考察,结果良好。 Objective To prepare melittin perfluorocarbon(PFC) nanocapsules(NPs) and investigate the particle size,Zeta potential,morphology of electron microscopy(EM),entrapment efficiency and stability.Methods Melittin loaded within PFC NPs were constructed by high pressure homogeneous processing method.The morphology and size of NPs were detected by transmission electron microscopy(TEM) and laser particle size analyzer.Drug entrapment efficiency was assessed by two-colorimetric Coomassie brilliant blue.The stability of melittin PFC NPs was investigated by evaluating the change of its average particle size and entrapment efficiency during storage at 4℃for 30 days.Results The average particle size of melittin PFC NPs was 84.41 nm,polydispersity was 0.115,Zeta potential was-52.1 mV.The linear range of melittin was 0.5~25 mg/L(r=0.999 3).Entrapment efficiency of three batches of melittin PFC NPs was(86.31±0.76)%(n=3) with RSD less than 1%.Conclusion It is feasible that melittin loaded within PFC NPs can be constructed by high pressure homogeneous processing method.The investigation results are good by the particle size,morphology of EM and entrapment efficiency.
出处 《安徽医科大学学报》 CAS 北大核心 2011年第9期909-912,共4页 Acta Universitatis Medicinalis Anhui
基金 国家自然科学基金(编号:30973917) 安徽医科大学省部级重点实验室培育计划(编号:SBSYS-0803)
关键词 蜂毒肽 纳米囊 melittin nanocapsules
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  • 1Shi-Ting Bao, Shui-Qing Gui and Mu-Sheng Lin Department of Hepatobiliary Surgery, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, China.Relationship between expression of Smac and Survivin and apoptosis of primary hepatocellular carcinoma[J].Hepatobiliary & Pancreatic Diseases International,2006,5(4):580-583. 被引量:28
  • 2胡海洋,陈大为,张春叶.蜂毒多肽长循环脂质体的制备研究[J].中国药学杂志,2005,40(15):1160-1163. 被引量:9
  • 3侯冬枝,刘长科,平其能,梁晓辉.牛血清白蛋白脂质体包封率的测定方法研究[J].药学学报,2007,42(5):545-549. 被引量:11
  • 4RIESS JG. Understanding the fundamentals of perfluorocarbons and perfluorocarbon emulsions relevant to in vivo oxygen delivery [J]. Artif Cells Blood Substit hnmobil Biotechnol, 2005, 33 (1): 47-63.
  • 5MULDER WJ, STRIJKERS GJ, GRIFFIOEN AW, et ol. A liposomal system for contrast-enhanced magnetic resonance imaging of molecular targets[J]. Bioeonjug Chem, 2004, 15 (4) : 799-806.
  • 6HAMILTON MC, PEEK GJ, DUX AE. Partial liquid ventilation [J]. Pediatr Radiol, 2005, 35 ( 11 ) : 1152-1156.
  • 7LANZA GM, WINTER P, CARUTHERS S, et al. Novel paramagnetic contrast agents for molecular imaging and targeted drug delivery[J]. Curr Pharm Biotechnol, 2004, 5(6): 495-507.
  • 8LANZA GM, WALLACE KD, SCOTT MJ, et al. A novel sitetargeted ultrasonic contrast agent with broad biomedical application[J]. Circulation, 1996, 94(12) : 3334-3340.
  • 9LANZA GM, YU X, WINTER PM. Targeted antiproliferative drug delivery to vascular smooth muscle cells with a magnetic resonance imaging nanoparticle contrast agent [J]. Circulation, 2002, 106(22): 2842-2847.
  • 10GUZMAN LA, LABHASETWAR V, SONG C. et ol. Local intraluminal infusion of biodegradable polymeric nanoparticles. A novel approach for prolonged drug delivery after balloon angioplasty[J]. Circulation, 1996, 94(6): 1441-1448.

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